HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339343Generated: October 30, 2026
3-amino-4-hydroxy-N-(1-propylbutyl)benzamide → N-(heptan-4-yl)-2-(methylthio)benzo[d]oxazole-5-carboxamide
https://huagongshe.com/reaction/339343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-amino-4-hydroxy-N-(1-propylbutyl)benzamide | HCID 66773120 | — |
| Reactant | N-(Heptan-4-yl)-2-(mercapto)benzo[d]oxazole-5-carboxamide | HCID 178443996 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(heptan-4-yl)-2-(methylthio)benzo[d]oxazole-5-carboxamide | HCID 57528011 | 55% |
Reaction Steps
N-(Heptan-4-yl)-2-(mercapto)benzo[d]oxazole-5-carboxamide: To a solution 3-amino-4-hydroxy-N-(1-propylbutyl)benzamide (example 41a) (250 mg, 1.0 mmol) in EtOH was added KSCSOEt (160 mg, 1.0 mmol). The resulting reaction mixture was heated at 80° C. overnight. The solvent was removed under reduced pressure. And the residue was taken up in water. The resulting mixture was acidified with HOAc to pH ˜5 and then filtered. The residue was washed with water to afford the product as a white solid (160 mg, 55%). MS (M+H, 293.1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895050B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-91914baf27bd4fb09880c9ae808d1015 |
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| Source note | uspto-grants-2014_11 |
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